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  • Search Condition : Filter (MeSH = Retinal Degeneration / pathology)
Species Resource
Drosophila Self-assembly of FUS through its low-complexity domain contributes to neurodegeneration.
Drosophila RNA binding mediates neurotoxicity in the transgenic Drosophila model of TDP-43 proteinopathy.
Mice B6.129S-Atg5<tm1Myok>(RBRC02975) , B6.Cg-Atg7<tm1Tchi>(RBRC02759) Early AMD-like defects in the RPE and retinal degeneration in aged mice with RPE-specific deletion of Atg5 or Atg7.
Drosophila 9553R-3 Familial Amyotrophic Lateral Sclerosis-linked Mutations in Profilin 1 Exacerbate TDP-43-induced Degeneration in the Retina of Drosophila melanogaster through an Increase in the Cytoplasmic Localization of TDP-43.
Human and Animal Cells Retinal pigmented epithelial cells obtained from human induced pluripotent stem cells possess functional visual cycle enzymes in vitro and in vivo.
Rats RCS/Kyo (strainID=27) Safety and Efficacy of Human Wharton's Jelly-Derived Mesenchymal Stem Cells Therapy for Retinal Degeneration.
Zebrafish Tg(zfRh1-3.7B:EGFP)/kj2 , Tg(zfSWS1-5.5A:EGFP)/kj9 Longitudinal fluorescent observation of retinal degeneration and regeneration in zebrafish using fundus lens imaging.
Mice B6;129-Grn<tm1>(RBRC02370) Progressive retinal degeneration and accumulation of autofluorescent lipopigments in Progranulin deficient mice.